Primary Device ID | 00763000185145 |
NIH Device Record Key | 6039448a-8d8d-49d3-92da-c4e7c5e53301 |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | FP6000L |
Company DUNS | 006261481 |
Company Name | MEDTRONIC, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00763000185145 [Primary] |
MHY | Stimulator, electrical, implanted, for parkinsonian tremor |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-07-20 |
Device Publish Date | 2020-07-12 |
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